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WO2018196639A1 - Procédé de lutte contre la croissance de végétaux résistants à l'als - Google Patents

Procédé de lutte contre la croissance de végétaux résistants à l'als Download PDF

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Publication number
WO2018196639A1
WO2018196639A1 PCT/CN2018/083141 CN2018083141W WO2018196639A1 WO 2018196639 A1 WO2018196639 A1 WO 2018196639A1 CN 2018083141 W CN2018083141 W CN 2018083141W WO 2018196639 A1 WO2018196639 A1 WO 2018196639A1
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WIPO (PCT)
Prior art keywords
spp
metribuzin
als
plants
triazolopyrimidine sulfonanilides
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Application number
PCT/CN2018/083141
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English (en)
Inventor
James Timothy Bristow
Original Assignee
Rotam Agrochem International Company Limited
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Publication date
Application filed by Rotam Agrochem International Company Limited filed Critical Rotam Agrochem International Company Limited
Priority to CN201880014014.5A priority Critical patent/CN110381737B/zh
Publication of WO2018196639A1 publication Critical patent/WO2018196639A1/fr

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Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/707—1,2,3- or 1,2,4-triazines; Hydrogenated 1,2,3- or 1,2,4-triazines
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system

Definitions

  • the present invention relates to a method of controlling the growth of ALS-tolerant plants.
  • Triazolopyrimidine sulfonanilide herbicides are acetolactate synthase (ALS) inhibitors. The compounds act by inhibiting biosynthesis of the essential amino acids valine and isoleucine, thereby stopping cell division in the plant and plant growth.
  • Metribuzin (IUPAC name: 4-amino-6-tert-butyl-4, 5-dihydro-3-methylthio-1, 2, 4-triazin-5-one; 4-amino-6-tert-butyl-3-methylthio-1, 2, 4-triazin-5 (4H) -one) is a triazinone herbicide and has the following chemical structure:
  • Metribuzin is an inhibitor of photosynthesis in plants.
  • the compound can be absorbed by roots and leaves of the plants and then translocate in the xylem.
  • Metribuzin is active in the control of grasses and broad-leaved weeds.
  • Metribuzin is commercially available in herbicidal compositions and methods for its preparation are known in the art.
  • a combination of metribuzin with one or more triazolopyrimidine sulfonanilides provides an effective treatment for ALS-tolerant plants and allows the plant growth to be controlled.
  • the combination of metribuzin and one or more triazolopyrimidine sulfonanilides displays a synergistic effect in the control of ALS-tolerant plants and exhibits an activity that is significantly greater than the activity of metribuzin alone or the level of activity expected from the combination of the individual active ingredients.
  • the present invention provides a method for the control of the growth of ALS-tolerant plants, the method comprising applying to the plants and/or their locus a herbicidally effective amount of a combination of (A) metribuzin and (B) one or more triazolopyrimidine sulfonanilides.
  • the present invention provides the use of a herbicidally effective amount of a combination of (A) metribuzin and (B) one or more triazolopyrimidine sulfonanilides in the control of the growth of ALS-tolerant plants.
  • the present invention also provides a composition for the control of ALS-tolerant plants comprising a herbicidally effective amount of a combination of (A) metribuzin and (B) one or more triazolopyrimidine sulfonanilides.
  • herbicide refers to a compound that exhibits activity in the control of the growth of plants.
  • herbicidally effective amount refers to the quantity of such a compound or combination of such compounds that is capable of producing a controlling effect on the growth of plants.
  • a controlling effect includes all deviations from the natural development and growth of the plant, including, for example, killing the plant, retardation of one or more aspects of the development and growth of the plant, leaf burn, albinism, dwarfing and the like.
  • plants refers to all physical parts of a plant, including shoots, leaves, needles, stalks, stems, fruit bodies, fruits, seeds, roots, tubers and rhizomes.
  • the abbreviation of the "common name” of the herbicides is used in the present specification, it is to be understood as including all conventional derivatives, such as the esters, in particular the lower alkyl esters, especially the methyl ester, and salts, and isomers, in particular the optical isomers, and all commercially available form or forms of the compound. If the "common name” refers to an ester or salt, this also includes all of the other usual derivatives, such as other esters and salts, the free acids, neutral compounds and isomers, in particular optical isomers, and all commercially available forms.
  • the present invention employs a combination of (A) metribuzin and (B) one or more triazolopyrimidine sulfonanilides.
  • the invention may employ a single triazolopyrimidine sulfonanilide.
  • the invention may employ a plurality of different triazolopyrimidine sulfonanilides, for example a mixture of 2, 3 or more triazolopyrimidine sulfonanilides as component (B) .
  • component (B) is a single triazolopyrimidine sulfonanilides.
  • metribuzin is a known herbicidal compound and is available commercially.
  • Suitable herbicidal triazolopyrimidine sulfonanilides for use in the present invention are known in the art and are commercially available.
  • Suitable triazolopyrimidine sulfonanilides for use in component (B) include one or more of cloransulam, diclosulam, florasulam, flumetsulam, metosulam, penoxsulam and pyroxsulam.
  • Preferred triazolopyrimidine sulfonanilides are florasulam, diclosulam, flumetsulam, penoxsulam, and mixtures of two, three or all thereof.
  • component (B) comprises florasulam.
  • the present invention employs a combination of metribuzin and a single triazolopyrimidine sulfonanilide florasulam.
  • the application rate of the active ingredients (A) metribuzin and (B) one or more triazolopyrimidine sulfonanilides depends on such factors as the type of weed, type of crop plant, soil type, season, climate, soil ecology and various other factors.
  • the application rate of the components for a given set of conditions can readily be determined by routine trials.
  • the components (A) metribuzin and (B) one or more triazolopyrimidine sulfonanilides can be applied at an application rate of from about 0.02 kilograms/hectare (kg/ha) to about 2 kg/ha of the total amount of active ingredients being applied.
  • the application rate is from about 0.05 kg/ha to about 1.5 kg/ha of the total amount of active ingredients.
  • Metribuzin may be applied in an amount of at least 5 g/ha, preferably at least 10 g/ha, more preferably at least 15 g/ha, still more preferably at least 20 g/ha. Metribuzin may be applied at an application rate of up to 600 g/ha, preferably up to 500 g/ha, more preferably up to 400 g/ha, more preferably still up to 300 g/ha. For many embodiments an application rate of up to 100 g/ha is very suitable. In some preferred embodiments, metribuzin is applied in an amount of 80 g/ha.
  • the one or more triazolopyrimidine sulfonanilides may be applied in a total amount of at least 1 g/ha, preferably at least 1.5 g/ha, more preferably at least 2 g/ha. In many embodiments, an application rate of at least 3 g/ha is very suitable, more preferably at least 4 g/ha.
  • the one or more triazolopyrimidine sulfonanilides may be applied in a total amount of up to 200 g/ha, preferably up to 150 g/ha, more preferably up to 125 g/ha, still more preferably up to 100 g/ha.
  • an application rate of from 3 g/ha to 70 g/ha is very suitable, more preferably from 4 to 60 g/ha, still more preferably from 5 to 50 g/ha.
  • An application rate of up to 40 g/ha of the one or more triazolopyrimidine sulfonanilides is preferred for many embodiments.
  • the synergistic effects of (A) metribuzin and (B) one or more triazolopyrimidine sulfonanilides when combined or used together are exhibited in a wide range of weight ratios of the two components.
  • the components (A) and (B) may be applied in similar or equal amounts.
  • Component (B) one or more triazolopyrimidine sulfonanilides, may be applied in larger amounts by weight than component (A) , metribuzin. More preferably for many embodiments, component (A) metribuzin is applied in a higher amount by weight than component (B) one or more triazolopyrimidine sulfonanilides.
  • the weight ratio of (A) metribuzin and (B) one or more triazolopyrimidine sulfonanilides preferably is up to 400: 1, more preferably up to 300: 1, still more preferably up to 200: 1, more preferably still up to 150: 1, with a ratio up to 70: 1 being preferred in many embodiments.
  • a weight ratio of (A) metribuzin to (B) one or more triazolopyrimidine sulfonanilides of up to 50: 1 is very suitable, preferably up to 40: 1, for example up to 20: 1.
  • the weight ratio of (A) metribuzin and (B) one or more triazolopyrimidine sulfonanilides is preferably greater than 1: 20, more preferably greater than 1: 10, still more preferably greater than 1: 5, more preferably still greater than 1: 2, with a ratio of greater than 1: 1 being suitable for many embodiments.
  • the weight ratio of metribuzin to triazolopyrimidine sulfonanilide preferably lies within the range of from 1: 5 to 300: 1.
  • the weight ratio of (A) metribuzin and (B) one or more triazolopyrimidine sulfonanilides is from about 1: 4 to about 250: 1, more preferably from about 1: 1 to about 200: 1, still more preferably from about 1: 1 to about 100: 1, more preferably still from about 1: 1 to about 70: 1.
  • the weight ratio of (A) metribuzin to (B) one or more triazolopyrimidine sulfonanilides is from 1: 1 to 50: 1, preferably from 1: 1 to 20: 1, still more preferably from 1: 1 to 16: 1.
  • the components (A) metribuzin and (B) one or more triazolopyrimidine sulfonanilides may be applied to the plants and/or their locus simultaneously and/or consecutively.
  • the components may be employed in the form of separate formulations.
  • the components (A) and (B) may be employed as a mixture in a single formulation.
  • the components (A) metribuzin and (B) one or more triazolopyrimidine sulfonanilides may be applied at any stage in the growth of the plants to be controlled.
  • the components may be applied to a locus pre-emergence, for example as a soil treatment.
  • the components may be applied post-emergence of the plants to be controlled, for example as a foliar application or a soil treatment.
  • the present invention has been found to be particularly effective in the control of a range of ALS-resistant plants when applied post-emergence.
  • the components (A) metribuzin and (B) one or more triazolopyrimidine sulfonanilides may be applied to the plants or their locus once. Alternatively, the components may be applied a plurality of times. Particularly effective control of undesirable plants has been achieved using just a single application of the components or two applications spaced apart in time.
  • the combination of (A) metribuzin and (B) one or more triazolopyrimidine sulfonanilides is useful in treating a range of crops, including cereals, for example wheat, including both soft wheat and durum wheat, barley, rye, oats, maize, rice, sorghum, triticale and related crops; fruit, such as pomes, stone fruit and soft fruit, for example apples, grapes, pears, plums, peaches, almonds, cherries, and berries, for example strawberries, raspberries and blackberries; leguminous plants, for example beans, lentils, peas, soybeans, and peanuts; oil plants, for example rape, mustard, and sunflowers; cucurbitaceae, for example marrows, cucumbers, and melons; fibre plants, for example cotton, flax, hemp, and jute; citrus fruit, for example oranges, lemons, grapefruit and mandarins; vegetables, for example spinach, lettuce, asparagus, cabbages, carrots, onions, tomatoes, potatoes, and
  • the present invention is used for controlling growth of undesirable plants in cereals, leguminous plants, fibre plants and vegetables, more preferably in wheat, including both soft wheat and durum wheat, barley, rye, oats, maize, rice, sorghum, triticale, beans, lentils, peas, soybeans, and peanuts, cotton, flax, hemp, jute, spinach, lettuce, asparagus, cabbages, carrots, onions, tomatoes, potatoes, and paprika, more preferably in wheat, including both soft wheat and durum wheat, barley, rye, oats, triticale, maize, rice, soybeans, cotton, tomatoes and potatoes.
  • wheat including both soft wheat and durum wheat, barley, rye, oats, triticale, maize, rice, soybeans, cotton, tomatoes and potatoes.
  • the present invention has been found to be particularly effective in the control of undesirable ALS-tolerant plants in wheat, including both soft wheat and durum wheat, barley, rye, oats, maize and triticale.
  • Suitable crops that may be treated include those which are tolerant to metribuzin and triazolopyrimidine sulfonanilides.
  • the tolerance can be a natural tolerance produced by selective breeding or can be artificially introduced by genetic modification of the crop plants.
  • ‘tolerance’ means a low susceptibility to damage caused by one or more particular herbicides, in the present case metribuzin and triazolopyrimidine sulfonanilides.
  • ALS-tolerant plants that may be controlled include broadleaved weeds, grasses and sedges, for example, Abutilon spp.; Acalypha spp.; Acanthospermum spp.; Agrostemma spp.; Alopecurus spp.; Amaranthus spp.; Ambrosia spp.; Amsinckia spp.; Anoda spp.; Anthemis spp.; Asperugo spp.; Atriplex spp.; Avena spp.; Boraginaceae spp.; Brachiaria spp.; Brassica spp.; Bromus spp.; Camelina spp.; Capsella spp.; Cardamine spp.; Cassia s
  • (A) metribuzin and (B) one and more triazolopyrimidine sulfonanilides is particularly effective in the control of the following plants which have developed ALS-tolerant varieties: Velvetleaf (Abutilon theophrasti) ; Hophornbeam Copperleaf (Acalypha ostryifolia) ; Bristly Starbur (Acanthospermum hispidum) ; Corncockle (Agrostemma githago) ; Blackgrass (Alopecurus myosuroides) ; Pigweeds (Amaranthus spp.
  • Cupgrass Eriochloa gracilis
  • Filaree Redstem (Erodium cicutarium) ; Dogfennel (Eupatorium capillifolium) ;
  • Spurge Sun (Euphorbia helioscopia) ; Spotted Spurge (Euphorbia maculata) ;
  • Black-bindweed Fallopia convolvulus
  • Fumitory Fumaria officinalis
  • Hemp-nettle Galeopsis
  • Galinsoga Galinsoga spp.
  • Cleavers Galium aparine
  • Crane's-bill Geranium
  • Geranium Geranium spp.
  • Green foxtail (Setaria viridis) ; Russian Thistle (Sida spinosa) ; Charlock (Sinapis arvensis) ; Tumble mustard (Jim Hill) (Sisymbrium altissimum) ; Prickly Sida/Teaweed (Slda spinosa) ; Black Nightshade (Solanum nigrum) ; Buffalobur (Solanum rostratum) ; Smooth sow-thistle (Sonchus oleraceus) ; Shattercane (Sorghum bicolor) ; Seedling Johnsongrass (Sorghum halepense) ; Volunteer sorghum, (Sorghum spp.
  • ALS-tolerant plants that may be controlled very well by the present invention include Stellaria spp., Papaver spp. and Galium spp.
  • Specific species of plants that have developed ALS-tolerance and may be controlled include Stellaria media, Papaver rhoeas, and Galium aparine.
  • components (A) metribuzin and (B) one or more triazolopyrimidine sulfonanilides may be employed in the form of one or more compositions containing the active ingredients.
  • compositions of the active components used in the present invention can be formulated in conventional manner, for example by mixing metribuzin and/or one and more triazolopyrimidine sulfonanilides with appropriate auxiliaries.
  • auxiliaries will depend upon such factors as the type of formulation and the end use. Suitable auxiliaries are commercially available and will be known to the person skilled in the art.
  • the composition may comprise one or more auxiliaries selected from extenders, carriers, surfactants, stabilizers, anti-foaming agents, anti-freezing agents, preservatives, antioxidants, colorants, thickeners, solid adherents, fillers, wetting agents, dispersing agents, lubricants, anticaking agents and diluents.
  • auxiliaries selected from extenders, carriers, surfactants, stabilizers, anti-foaming agents, anti-freezing agents, preservatives, antioxidants, colorants, thickeners, solid adherents, fillers, wetting agents, dispersing agents, lubricants, anticaking agents and diluents.
  • auxiliaries are known in the art and are commercially available. Their use in the formulation of compositions for use in the present invention will be apparent to the person skilled in the art.
  • Suitable formulations for applying the combination of metribuzin and one or more triazolopyrimidine sulfonanilides include water-soluble concentrates (SL) , emulsifiable concentrates (EC) , oil in water emulsions (EW) , micro-emulsions (ME) , suspension concentrates (SC) , oil-based suspension concentrates (OD) , flowable suspensions (FS) , water-dispersible granules (WDG) , water-soluble granules (SG) , wettable powders (WP) , water soluble powders (SP) , granules (GR) , encapsulated granules (CG) , fine granules (FG) , macrogranules (GG) , aqueous suspo-emulsions (SE) , capsule suspensions (CS) and microgranules (MG) .
  • water-soluble concentrates SL
  • EC emulsif
  • compositions to be used in the present invention are suspension concentrates (SC) , and oil-based suspension concentrates (OD) .
  • compositions may comprise one or more inert fillers.
  • inert fillers are known in the art and available commercially.
  • Suitable fillers include, for example, natural ground minerals, such as kaolins, aluminas, talc, chalk, quartz, attapulgite, montmorillonite, and diatomaceous earth, or synthetic ground minerals, such as highly dispersed silicic acid, aluminum oxide, silicates, and calcium phosphates and calcium hydrogen phosphates.
  • Suitable inert fillers for granules include, for example, crushed and fractionated natural minerals, such as calcite, marble, pumice, sepiolite, and dolomite, or synthetic granules of inorganic and organic ground materials, as well as granules of organic material, such as sawdust, coconut husks, corn cobs, and tobacco stalks.
  • compositions may include one or more surfactants, which are preferably non-ionic, cationic and/or anionic in nature, and surfactant mixtures which have good emulsifying, dispersing and wetting properties, depending upon the active compound/compounds being formulated.
  • surfactants are known in the art and are commercially available.
  • Suitable anionic surfactants can be both so-called water-soluble soaps and water-soluble synthetic surface-active compounds.
  • Soaps which may be used include the alkali metal, alkaline earth metal or substituted or unsubstituted ammonium salts of higher fatty acids (C 10 to C 22 ) , for example the sodium or potassium salt of oleic or stearic acid, or of natural fatty acid mixtures.
  • the surfactant system may comprise an emulsifier, dispersant or wetting agent of ionic or nonionic type.
  • surfactants include salts of polyacrylic acids, salts of lignosulphonic acid, salts of phenylsulphonic or naphthalenesulphonic acids, polycondensates of ethylene oxide with fatty alcohols or with fatty acids or with fatty amines, substituted phenols, especially alkylphenols, sulphosuccinic ester salts, taurine derivatives, especially alkyltaurates, and phosphoric esters of polyethoxylated phenols or alcohols.
  • the presence of at least one surfactant is generally required when the active compound and/or the inert carrier and/or auxiliary/adjuvant are insoluble in water and the vehicle for the final application of the composition is water.
  • compositions optionally further comprise one or more polymeric stabilizers.
  • Suitable polymeric stabilizers that may be used in the present invention include, but are not limited to, polypropylene, polyisobutylene, polyisoprene, copolymers of monoolefins and diolefins, polyacrylates, polystyrene, polyvinyl acetate, polyurethanes or polyamides. Suitable stabilizers are known in the art and are commercially available.
  • surfactants and polymeric stabilizers mentioned above are generally believed to impart stability to the compositions, in turn allowing the compositions to be formulated, stored, transported and applied.
  • Suitable anti-foaming agents include all substances which can normally be used for this purpose in agrochemical compositions. Suitable anti-foaming agents are known in the art and are available commercially. Particularly preferred anti-foaming agents include modified polydimethylsiloxane formulations, such as SAG 1529 from Momentive, modified polyether-polysiloxanes, such as AF9902 from Evonik, mixtures of polydimethylsiloxanes and perfluoroalkylphosphonic acids, such as the silicone anti-foaming agents commercially available from GE or Compton.
  • modified polydimethylsiloxane formulations such as SAG 1529 from Momentive
  • modified polyether-polysiloxanes such as AF9902 from Evonik
  • mixtures of polydimethylsiloxanes and perfluoroalkylphosphonic acids such as the silicone anti-foaming agents commercially available from GE or Compton.
  • Suitable preservatives for use in the compositions include all substances which can normally be used for this purpose in agrochemical compositions of this type and again are well known in the art. Suitable examples that may be mentioned include the commercially available preservatives (from Bayer AG) and (from Bayer AG) and NIPACIDE BIT 20 (from Clariant) .
  • Suitable antioxidants for use in the compositions are all substances which can normally be used for this purpose in agrochemical compositions, as is known in the art. Preference is given to butylated hydroxytoluene.
  • Suitable thickeners for use in the compositions include all substances which can normally be used for this purpose in agrochemical compositions, for example xanthan gum, PVOH, cellulose and its derivatives, clay hydrated silicates, magnesium aluminum silicates or a mixture thereof. Again, such thickeners are known in the art and are available commercially.
  • compositions may further comprise one or more solid adherents.
  • adherents are known in the art and available commercially. They include organic adhesives, including tackifiers, such as celluloses or substituted celluloses, natural and synthetic polymers in the form of powders, granules, or lattices, and inorganic adhesives such as gypsum, silica, or cement.
  • the combination of the active ingredients (A) metribuzin and (B) one or more triazolopyrimidine sulfonanilides can be applied to the plants, such as to the leaves of plants, and/or to their locus where control is desired, such as to the surrounding soil, by any convenient method.
  • locus refers to the place where plants are growing, the place where the plant propagation materials of plants are sown or the place where the plant propagation materials of plants will be sown.
  • Suitable methods for applying the components are known in the art and include coating, spraying, sprinkling, dipping, soaking, injection, irrigation, and the like.
  • the method of the present invention may employ other pesticides, in addition to the combination of (A) metribuzin and (B) one or more triazolopyrimidine sulfonanilides.
  • compositions employed in the present invention may contain or be mixed with other pesticides or other active components, such as fungicides, insecticides and nematicides, growth factor enhancers and fertilizers, to enhance the activity of the treatment of the present invention or to widen its spectrum of activity.
  • the method of the present invention may be employed in conjunction with the use of one or more of the aforementioned active ingredients, again to obtain an enhanced efficacy or broader spectrum of activity.
  • a suspension concentrate (SC) formulation was prepared from the components summarized in Table 1 below.
  • An oil-based suspension concentrate (OD) formulation was prepared from the components summarized in Table 2 below.
  • the expected activity for a given combination of two active compounds can be calculated by the so called “Colby equation” (see S.R. Colby, “Calculating Synergistic and Antagonistic Responses of Herbicide Combinations” , Weeds 1967, 15, 20-22) :
  • A the activity percentage of compound A when active compound A is employed at an application rate of m g/ha;
  • E the percentage of estimated activity when compounds A and B are employed together at an application rate of m g/ha and n g/ha.
  • Examples C1 to C5 and 1 to 9 were tested for their biological activity against ALS-tolerant plants, in particular plants exhibiting resistance to triazolopyrimidine sulfonanilides, as follows:
  • Seeds of a normal wild variety and an ALS-resistant variant of each of Stellaria media, Papaver rhoeas, and Galium aparine were sown in trays of peat-based compost placed in a glasshouse to allow germination.
  • four evenly sized seedlings were each transplanted into 9 cm diameter plastic pots containing loam soil mixed with 25%by volume horticultural silver sand and further blended with coarse grit in the ratio 3: 1.
  • the resulting potting medium was supplemented with Osmacote slow-release fertilizer (16: 8: 9 + Mg) in an amount sufficient to provide 1.4 g per 0.35 L pot.
  • the plants were returned to the glasshouse and the sprayed pots were arranged in three randomized blocks.
  • the temperature of the glasshouse ranged from 12.2°C to 16.1°C by day and 10.9°C to 13.3°C at night.
  • the relative humidity ranged from 75 %to 101 %.
  • the plants were watered to maintain the soil close to the field capacity. Following herbicide treatment, the plants were watered by sub-irrigation using individual plastic dishes for each pot to avoid any risk of cross contamination.
  • the visual percentage of control based on a 0 –100 linear scale was assessed 21 days after treatment (DAT) .
  • the linear scale ranged from 0 (no effect) to 100 (dead plants) .
  • the triazolopyrimidine sulfonanilides had little or no effect on all ALS-tolerant plants (compositions C2 to C5) , while significantly damaging the wild (non-tolerant) plants.

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  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
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  • Wood Science & Technology (AREA)
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  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

La présente invention concerne un procédé de lutte contre la croissance de végétaux résistants à l'ALS, ledit procédé consistant à appliquer sur les végétaux, et/ou sur leur emplacement, une quantité efficace du point de vue herbicide d'une combinaison de (A) métribuzine et (B) d'un ou plusieurs sulfonanilides de triazolopyrimidine. L'invention concerne également l'utilisation d'une quantité efficace du point de vue herbicide d'une combinaison de (A) métribuzine et (B) d'un ou plusieurs sulfonanilides de triazolopyrimidine dans la lutte contre la croissance de végétaux résistants à l'ALS. L'invention concerne également une composition pour la lutte contre les végétaux résistants à l'ALS comprenant une quantité efficace du point de vue herbicide d'une combinaison de (A) métribuzine et (B) d'un ou plusieurs sulfonanilides de triazolopyrimidine.
PCT/CN2018/083141 2017-04-25 2018-04-16 Procédé de lutte contre la croissance de végétaux résistants à l'als WO2018196639A1 (fr)

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CN201880014014.5A CN110381737B (zh) 2017-04-25 2018-04-16 控制als耐受性植物生长的方法

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EP17167944.2 2017-04-25
EP17167944.2A EP3395173A1 (fr) 2017-04-25 2017-04-25 Procédé de régulation de la croissance de plantes tolérantes aux als

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* Cited by examiner, † Cited by third party
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WO2012135441A1 (fr) * 2011-03-30 2012-10-04 Dow Agrosciences Llc Le pénoxsulam comme herbicide pour la luzerne
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